Czitrom A A, Edwards S, Phillips R A, Bosma M J, Marrack P, Kappler J W
J Immunol. 1985 Apr;134(4):2276-80.
We have examined the antigen-presenting function of spleen cells in the C.B-17 scid mouse, a mutation that severely impairs the development of T and B lymphocytes. We show that antigen-presenting cells (APC) of SCID mice function normally in antigen-specific proliferative responses of primed T cells and in the antigen-specific activation of IL 2-producing T cell hybridomas. In both quantitative and qualitative terms, APC of SCID mice are equivalent to those of normal mice. These results indicate that the development and differentiation of APC function in vivo is independent of signals from mature, functional T or B lymphocytes.
我们研究了C.B-17 scid小鼠脾细胞的抗原呈递功能,该小鼠发生的突变严重损害了T和B淋巴细胞的发育。我们发现,SCID小鼠的抗原呈递细胞(APC)在致敏T细胞的抗原特异性增殖反应以及产生白细胞介素2的T细胞杂交瘤的抗原特异性激活中功能正常。在数量和质量方面,SCID小鼠的APC与正常小鼠的APC相当。这些结果表明,APC在体内的功能发育和分化独立于成熟的、功能性T或B淋巴细胞发出的信号。